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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1848745 | Oliver-McFarlane syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0442874 | Neuropathy | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011882 | Diabetic Neuropathies | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C3714756 | Intellectual Disability | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0020758 | Congenital ichthyosis | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0020757 | Ichthyoses | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0271683 | Polyneuropathy, Motor | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0917799 | Hypersomnia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0270763 | Familial Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0009714 | Hepatic Fibrosis, Congenital | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0085084 | Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0011570 | Mental Depression | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0037050 | Sick Building Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C1854520 | SEBASTIAN SYNDROME | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0022735 | Klinefelter Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0085636 | Photophobia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0235991 | Small for gestational age (disorder) | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0339537 | Cone monochromatism | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0037772 | Spastic Paraplegia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0002736 | Amyotrophic Lateral Sclerosis | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0030567 | Parkinson Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C1857941 | Brooke-Spiegler syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0029124 | Optic Atrophy | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0342384 | Idiopathic hypogonadotropic hypogonadism | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
